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564-20-5

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  • High Quality 98% Sclareolide Perilla Frutescens Extract

    Cas No: 564-20-5

  • USD $ 280.0-290.0 / Kilogram

  • 1 Kilogram

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564-20-5 Usage

Chemical Properties

Sclareolide has a musky, wood odor.

Occurrence

Reported present in clary sage bush (Salvia sclarea)

Uses

Different sources of media describe the Uses of 564-20-5 differently. You can refer to the following data:
1. Sclareolide is found in Salvia yosgadensis and is a close analog of sclareol, an antifungal diterpene.
2. antimicrobial
3. sclareolide is a fragrancing ingredient, it can help mask formulation odors. It is synthetically manufactured.

Preparation

Sclareol, isolated from clary sage by solvent extraction, can be efficiently oxidized by the microorganism Cryptococcus albidus to sclareolide.

General Description

Sclareolide is a diterpenoid compound mainly used in the perfume industry for its amber like odor.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 564-20-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 564-20:
(5*5)+(4*6)+(3*4)+(2*2)+(1*0)=65
65 % 10 = 5
So 564-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H26O2/c1-14(2)7-5-8-15(3)11(14)6-9-16(4)12(15)10-13(17)18-16/h11-12H,5-10H2,1-4H3/t11-,12+,15-,16+/m0/s1

564-20-5 Well-known Company Product Price

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  • TCI America

  • (S0847)  (3aR)-(+)-Sclareolide  >97.0%(GC)

  • 564-20-5

  • 5g

  • 490.00CNY

  • Detail
  • TCI America

  • (S0847)  (3aR)-(+)-Sclareolide  >97.0%(GC)

  • 564-20-5

  • 25g

  • 1,390.00CNY

  • Detail
  • Sigma-Aldrich

  • (56699)  (3aR)-(+)-Sclareolide  analytical standard

  • 564-20-5

  • 56699-100MG

  • 568.62CNY

  • Detail
  • Aldrich

  • (358002)  (3aR)-(+)-Sclareolide  97%

  • 564-20-5

  • 358002-5G

  • 845.91CNY

  • Detail

564-20-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aR)-(+)-Sclareolide

1.2 Other means of identification

Product number -
Other names (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-1,4,5,5a,7,8,9,9b-octahydrobenzo[e][1]benzofuran-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:564-20-5 SDS

564-20-5Relevant articles and documents

Palladium-Catalyzed Low Pressure Carbonylation of Allylic Alcohols by Catalytic Anhydride Activation

Schelwies, Mathias,Paciello, Rocco,Pelzer, Ralf,Siegel, Wolfgang,Breuer, Michael

, p. 9263 - 9266 (2021/05/27)

A direct carbonylation of allylic alcohols has been realized for the first time with high catalyst activity at low pressure of CO (10 bar). The procedure is described in detail for the carbonylation of E-nerolidol, an important step in a new BASF-route to (?)-ambrox. Key to high activities in the allylic alcohol carbonylation is the finding that catalytic amounts of carboxylic anhydride activate the substrate and are constantly regenerated with carbon monoxide under the reaction conditions. The identified reaction conditions are transferrable to other substrates as well.

Chiral complementary alkyl heterocyclic compounds and their use as fungicides

-

Paragraph 0060-0064, (2020/10/20)

The invention relates to a chiral drimane heterocyclic compound and a purpose of the chiral drimane heterocyclic compound as a sterilizing agent. A chemical structural general formula of the compoundis shown as a formula (I), in the formula (I), 8-bit stereo configuration is R or S, and represents the heterocyclic compound, comprising iso-oxazoline, isoxazole, pyrazoline, pyrimidine, benzimidazole and pyrimidine, or diazepine.

Direct Decarboxylative Functionalization of Carboxylic Acids via O-H Hydrogen Atom Transfer

Na, Christina G.,Ravelli, Davide,Alexanian, Erik J.

supporting information, p. 44 - 49 (2020/01/22)

Decarboxylative functionalization via hydrogen atom transfer offers an attractive alternative to standard redox approaches to this important class of transformations. Herein, we report a direct decarboxylative functionalization of aliphatic carboxylic acids using N-xanthylamides. The unique reactivity of amidyl radicals in hydrogen atom transfer enables decarboxylative xanthylation under redox-neutral conditions. This platform provides expedient access to a range of derivatives through subsequent elaboration of the xanthate group.

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